Utilization of a unitary transform for efficient computation in the matrix pencil method to find the direction of arrival

In this study, we use the matrix pencil (MP) method to compute the direction of arrival (DOA) of the signals using a very efficient computational procedure in which the complexity of the computation can be reduced significantly by using a unitary matrix transformation. This method applies the technique directly to the data without forming a covariance matrix. Simulation results show that the variance of the estimate approaches to the Cramer-Rao lower bound. Using real computations through the unitary transformation for the MP method leads to a very efficient computational methodology for real time implementation on a digital signal processor chip. A unitary transform can convert the complex matrix to a real matrix along with their eigenvectors and thereby reducing the computational cost at least by a factor of four without sacrificing accuracy. This reduction in the number of computations is achieved by using a transformation, which maps centro-hermitian matrices to real matrices. This transformation is based on Lee's work on centro-hermitian matrices.     

A new design topology for low-voltage CMOS current feedback amplifiers

A new topology for designing low-voltage current feedback amplifiers (CFAs) is presented. By employing a second-generation positive current conveyor followed by an operational amplifier in an unconventional manner, the design circumvents the problem of trying to achieve large transimpedance in a low-voltage environment. It is shown that this CFA configuration also results in near gain independent closed-loop bandwidth defined by a single feedback resistor. The proposed amplifier was verified experimentally by a chip designed using Taiwan Semiconductor Manufacturing Company's 0.18-/spl mu/m digital CMOS process of a single-ended power supply of 1.8 V.     

Protein-Assembled Nanocrystal-Based Vertical Flash Memory Devices with Al<Subscript>2</Subscript>O<Subscript>3</Subscript> Integration

This work presents vertical flash memory devices with protein-assembled PbSe nanocrystals as a floating gate and Al₂O₃ as a control oxide. The advantage of a vertical structure is that it improves cell density. Protein assembly improves uniformity of nanocrystals, which reduces threshold voltage variation among devices. The introduction of Al₂O₃ as a control oxide provided lower voltage/faster operation and hence less power consumption compared with the devices fabricated with SiO₂. The integration of Al₂O₃ appeared to be compatible with the protein assembly approach. In conclusion, Al₂O₃ has the potential to become the high-k control oxide due to its relatively high electron/hole barrier heights, and high permittivity.     

An accurate, analytical, and technology-mapped definition of the surface potential at threshold and a new postulate for the threshold voltage of MOSFETs

A novel approach of defining the threshold voltage for long channel MOSFETs has been presented in this paper, where it has been proposed that it corresponds to the gate-to-source voltage for which the drift and diffusion components of the total drain current become equal to each other. In order to avoid the greater computation time associated with the numerical solution of these two components, an analytical expression of the surface potential, corresponding to the threshold condition, is given here, which has the same functional form as the one proposed by Tsividis. The fuzzy parameter n, appearing in this expression of the surface potential, is expressed as a function of the substrate doping density (N_A) and the oxide thickness (t_ox). The threshold voltage values, obtained analytically from the relation between the surface potential at the threshold condition and the closed-form technology-mapped expression of the fuzzy parameter n, show an excellent match with those obtained from SILVACO simulations for a wide range of N_A and t_ox, with the maximum error being only about 4%. The comparison of the percent error values of the threshold voltage obtained from this proposed model with those obtained from the other two recently proposed methods, all with respect to SILVACO simulation results, further verifies the validity of our completely analytical, mathematically simple, and straight-forward approach, proposed in this work here.     

Behavior of cellulose liquefaction after pretreatment using ionic liquids with water mixtures

Ionic liquid (IL)‐water mixtures were applied in cellulose pretreatment experiment and the pretreated cellulose was used in subsequent phenol liquefaction process as a new application method. Cellulose recovery rate and the average molecular weight (M_w) of pretreated cellulose were investigated to understand the influence of these mixtures on cellulose structure. X‐ray diffraction, Fourier transform infrared, gel permeation chromatograph, and scanning electron microscope were used to clarify the changes of pretreated cellulose. The liquefied residues from untreated cellulose and pretreated cellulose were considered as significant index to determine the effect of IL‐water mixtures on cellulose. Moreover, liquefied residues were initially characterized by the variation of the average M_w. It was suggested that the lower M_w of cellulose obtained in IL‐water mixtures, and the crystalline structure was disrupted. So, some cracks were found on the cellulose surface obviously. The liquefied residues result suggested that the pretreated cellulose obtained the lower residues at the same time or the same amount of residues by using the less time. The behavior of cellulose liquefaction efficiency using IL‐water mixture pretreatment was discussed. The lower M_w of cellulose was the major factor, which accelerates the cellulose phenol liquefaction process efficiency. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40255.     

In situ synthesis,fabrication and Rietveld refinement of the hydroxyapatite/titania composite coatings on 316 L SS

The development of Hydroxyapatite (HAP)/Titania (TiO₂) composite coatings on metallic implants have received a great deal of attention during the recent years owing to their superior advantages in biomedical applications. The present study has focused on the in situ formation of HAP/TiO₂ composite powders through aqueous precipitation technique. Five different HAP/TiO₂ composite powders of varied HAP to TiO₂ ratios has been synthesized in the present study and the results were compared with the stoichiometric HAP, Rutile TiO₂ and Anatase TiO₂ which also have been synthesized by adapting a similar synthetic procedure. All the synthesized powders have been analyzed using X-ray diffraction (XRD) and X-ray fluorescence (XRF) techniques. Rietveld Refinement technique has been employed to generate quantitative information about the structural characteristics and phase content in all the powder samples. Further, the electrophoretic deposition (EPD) method has been employed to fabricate HAP/TiO₂ composite coatings on 316 L SS and the resultant coatings were analyzed for its quantitative structural characteristics. The results from the present investigation has confirmed that concentration of TiO₂ in the HAP/TiO₂ composites and heat treatment temperatures have played a major role in the degradation of HAP to β-Tricalcium phosphate and also in the conversion of Anatase to Rutile TiO₂ phase.     

(Non-)Random Sequences from (Non-)Random Permutations—Analysis of RC4 Stream Cipher

RC4 has been the most popular stream cipher in the history of symmetric key cryptography. Its internal state contains a permutation over all possible bytes from 0 to 255, and it attempts to generate a pseudo-random sequence of bytes (called keystream) by extracting elements of this permutation. Over the last twenty years, numerous cryptanalytic results on RC4 stream cipher have been published, many of which are based on non-random (biased) events involving the secret key, the state variables, and the keystream of the cipher. Though biases based on the secret key are common in RC4 literature, none of the existing ones depends on the length of the secret key. In the first part of this paper, we investigate the effect of RC4 keylength on its keystream, and report significant biases involving the length of the secret key. In the process, we prove the two known empirical biases that were experimentally reported and used in recent attacks against WEP and WPA by Sepehrdad, Vaudenay and Vuagnoux in EUROCRYPT 2011. After our current work, there remains no bias in the literature of WEP and WPA attacks without a proof. In the second part of the paper, we present theoretical proofs of some significant initial-round empirical biases observed by Sepehrdad, Vaudenay and Vuagnoux in SAC 2010. In the third part, we present the derivation of the complete probability distribution of the first byte of RC4 keystream, a problem left open for a decade since the observation by Mironov in CRYPTO 2002. Further, the existence of positive biases towards zero for all the initial bytes 3 to 255 is proved and exploited towards a generalized broadcast attack on RC4. We also investigate for long-term non-randomness in the keystream, and prove a new long-term bias of RC4.     

Water table dynamics of Dhaka city and its long-term trend analysis using the “MAKESENS” model

The water table (WT) data of Dhaka city for 17 years (1988–2004) was analysed for assessing WT fluctuation and predicting its trend using a computer model, “MAKESENS”. The analysis revealed that the WT declined drastically at different locations of the city. Moreover, the model also predicted that WT would further decline 9–25 m by the year 2015 and 18–40 m by the year 2025, rendering most wells inoperative, if the pumping rate was not reduced.     

Fischer–Tropsch Synthesis: Morphology, Phase Transformation and Particle Size Growth of Nano-scale Particles

An unpromoted ultrafine iron nano-particle catalyst was used for Fischer–Tropsch synthesis (FTS) in a CSTR at 270 °C, 175 psig, H₂/CO = 0.7, and a syngas space velocity of 3.0 sl/h/g Fe. Prior to FTS, the catalyst was activated in CO for 24 h which converted the initial hematite into a mixture of 85% χ-Fe₅C₂ and 15% magnetite, as found by Mössbauer measurement. The activated catalyst results in an initial high conversion (ca. 85%) of CO and H₂; however the conversions decreased to ca. 10% over about 400 h of synthesis time and after that remained nearly constant up to 600 h. Mössbauer and EELS measurement revealed that the catalyst deactivation was accompanied by gradual in situ re-oxidation of the catalyst from initial nearly pure χ-Fe₅C₂ phase to pure magnetite after 400 h of synthesis time. Experimental data indicates that the nucleation for carbide/oxide transformation may initiates at the center of the particle by water produced during FTS. Small amount of ?′-Fe_2.2C phase was detected in some catalyst samples collected after 480 h of FTS which are believed to be generated by syngas during FTS. Particle size distribution (PSD) measurements indicate nano-scale growth of individual catalyst particle. Statistical average diameters were found to increase by a factor of 4 over 600 h of FTS. Large particles with the largest dimension larger than 150 nm were also observed. Chemical compositions of the larger particles were always found to be pure single crystal magnetite as revealed by EELS analysis. Small number of ultrafine carbide particles was identified in the catalyst samples collected during later period of FTS. The results suggest that carbide/oxide transformation and nano-scale growth of particles continues either in succession or at least simultaneously; but definitely not in the reverse order (in that case some larger carbide particles would have observed). EELS-STEM measurement reveals amorphous carbon rim of thickness 3–5 nm around some particles after activation and during FTS. Well ordered graphitic carbon layers on larger single crystal magnetite particles were found by EELS-STEM measurement. However the maximum thickness of the carbon (amorphous or graphitic) rim does not grow above 10 nm suggesting that the growths of particles are not due to carbon deposition.